CHD2 myoclonic encephalopathy is frequently associated with self-induced seizures
Published at : 04 Nov 2020
Objective: To delineate the phenotype of early childhood epileptic encephalopathy due to de novo mutations of CHD2, which encodes the chromodomain helicase DNA binding protein 2.
For more, see: http://www.neurology.org/content/84/9/951.short
Encephalopathy (Disease Or Medical Condition)Seizure (Symptom)Myoclonus (Symptom)